HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615570Generated: October 25, 2026
Hydrochloric Acid → tert-butyl N-{3-[(3-aminopropyl)(methyl)amino]propyl}carbamate
https://huagongshe.com/reaction/615570
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | N,N-bis(3-aminopropyl)methylamine | HCID 7777 | — |
| Reactant | O-(1,1-Dimethylethyl) S-(4,6-dimethyl-2-pyrimidinyl) carbonothioate | HCID 148428 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | tert-butyl N-{3-[(3-aminopropyl)(methyl)amino]propyl}carbamate | HCID 12983660 | 70.8% |
Reaction Steps
Into 180 ml of water, was dissolved 150 g of bis(3-aminopropyl)methylamine followed by 53 g of triethylamine. To the solution, while being cooled in ice and stirred, was added portionwise a solution of 83 g (1/3 equivalent) of 4,6-dimethyl-2-tert-butoxycarbonylthiopyrimidine in 200 ml of dioxane. The mixture was allowed to react at room temperature for 5 hours. The reaction mixture was stripped of the dioxane and triethyl amine by disillation under reduced pressure. The residue was adjusted to pH 2 with 6N hydrochloric acid and washed with chloroform. The aquoues layer was adjusted to pH 13.5 with sodium hydroxide and extracted with chloroform. The chloroform layer was dried over sodium sulfate and freed from the solvent by distillation under reduced pressure to yield 60 g (24% yield) of (3-tert-butoxycarbonylaminopropyl)-(3-aminopropyl)methylamine (BOC-APMP).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04500452 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-d4222fa452ae4fcd82b9c1b4812f7090 |
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| Source note | uspto-grants-1985_02 |
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