HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504834Generated: October 31, 2026
Hydrazine hydrate (1:1) → tert-butyl N-[1-amino-3-(methylsulfanyl)propan-2-yl]carbamate
https://huagongshe.com/reaction/1504834
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | tert-Butyl [2-phthalimido-1-(methylsulfanylmethyl)ethyl]carbamate | HCID 24720892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-butyl N-[1-amino-3-(methylsulfanyl)propan-2-yl]carbamate | HCID 72455593 | — |
Reaction Steps
To a solution of tert-butyl [1-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)-3-(methylsulfanyl)propan-2-yl]carbamate (from Step 3 of PrepEx 4.11) (10.0 g, 28.6 mmol) in ethanol (150 mL) was added dropwise hydrazine hydrate (15.7 g, 286 mmol) at 0° C. and then the reaction mixture was allowed to warm to ambient temperature. After 30 minutes, the reaction mixture was heated to reflux. After two hours, the reaction mixture was cooled, filtered, and concentrated under reduced pressure. The residue was purified by chromatography on silica gel to give tert-butyl [1-amino-3-(methylsulfanyl)propan-2-yl]carbamate. MS ESI calc'd. for C9H21N2O2S [M+H]+ 221. found 221. 1H NMR (400 MHz, CD3OD) δ 3.66-3.63 (m, 1H), 2.83-2.79 (m, 1H), 2.64-2.50 (m, 3H), 2.12 (s, 3H), 1.45 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216173B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-b40620f37a934282a7b5552bd37843b5 |
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| Source note | uspto-grants-2015_12 |
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