HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079244Generated: October 31, 2026
tert-Butyl 2-[(benzyloxy)methyl]piperazine-1-carboxylate → HCID 136121359, compound
https://huagongshe.com/reaction/2079244
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butyl 2-[(benzyloxy)methyl]piperazine-1-carboxylate | HCID 17750452 | — |
| Reactant | 2-(4-Chloro-7-methylquinazolin-2-yl)-phenol | HCID 136105032 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 136121359 | HCID 136121359 | 85% |
Reaction Steps
To a solution of 2-(4-chloro-7-methylquinazolin-2-yl)phenol (450 mg, 1.66 mmol) in 10 mL DMF was added a solution of (R)-tert-butyl 2-((benzyloxy)methyl)piperazine-1-carboxylate (610 mg, 1.99 mmol) in DMF and triethylamine (0.46 mL). The reaction mixture was then refluxed at 85° C. for 30 minutes, quenched with water, extracted twice with CH2Cl2, dried over Na2SO4, and concentrated to give (R)-tert-butyl 2-((benzyloxy)methyl)-4-(2-(2-hydroxyphenyl)-7-methylquinazolin-4-yl)piperazine-1-carboxylate (760 mg, 85%). This material was used in the next step without further purification. LC/MS: m/z 541.5 (M+H)+ at 3.37 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07928107B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-8e2f439dd2e746cfba4f317a7cba573d |
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| Source note | uspto-grants-2011_04 |
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