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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088718Generated: November 1, 2026

(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidine → 4-((R)-3-(methylamino)pyrrolidin-1-yl)-8-phenyl-5,6,7,8-tetrahydroquinazolin-2-amine

https://huagongshe.com/reaction/2088718

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R)-(+)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514397—
Reactanttert-Butyl methyl((3R)-pyrrolidin-3-yl)carbamateHCID 7019173—
Reactant2-amino-9,9-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[d]pyrimidin-4-yl 4-methylbenzenesulfonateHCID 86634880—
Product4-((R)-3-(methylamino)pyrrolidin-1-yl)-8-phenyl-5,6,7,8-tetrahydroquinazolin-2-amineHCID 44466871—

Reaction Steps

The title compound was prepared according to the procedures of Examples 1E and 1F, substituting the product from Example 9C for the product from Example 1D and substituting (R)-tert-butylmethyl(pyrrolidin-3-yl)carbamate for (R)-tert-butyl pyrrolidin-3-ylcarbamate. 1H NMR (300 MHz, CDCl3) δ 7.24 (m, 2H), 7.16 (t, J=7.29 Hz, 1H), 7.07 (d, J=7.12 Hz, 2H), 4.53 (s, 2H), 3.96 (t, J=6.27 Hz, 1H), 3.74 (m, 3H), 3.47 (m, 1H), 3.29 (m, 1H), 2.73 (m, 2H), 2.49 (d, J=2.71 Hz, 3H), 2.14 (m, 2H), 1.80 (m, 4H). MS (ESI+) m/z 324 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436005B2
Source datasetuspto-grants-2013_05
ORD IDord-85f223f3252c4322bf9f680e6a13903c
Source noteuspto-grants-2013_05